FDA label b17ff00f-b801-47fb-8034-8e85e32c318f

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
aa07ec60-45f3-485f-9188-38c0d50db12c
SPL ID
b17ff00f-b801-47fb-8034-8e85e32c318f
Version
4
Effective date
2021-06-01
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:40

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Cautions: 1. Stop using a product if you have any unusual symptoms mentioned below. Contacting with a dermatologist is recommended rather than using it continuously and making the symptom worse. 1) Red spots, swellings, itching, irritation. 2) Same symptoms as above occurred after the skin spot where you applied a product was exposed to direct sunlight. 2. Do not use for injured, eczema, or dermatitis spots. 3. Directions for storage and handling. 1) Remember to cover up a lid after using a product. 2) Keep a product in unreachable place from children. 3) Do not keep a product in too high or low temperature and under direct sunlight.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.